Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
107 participants
INTERVENTIONAL
2019-11-01
2024-10-17
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
SINGLE
Study Groups
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Multilevel Gaming Adherence
Participants in the intervention arm will receive Multilevel Gaming Adherence Intervention. Participants receive Battle Viro on their mobile phones, an electronic pill monitoring device, and, for 24 weeks, game-related text messages guided by medication adherence data (collected from an electronic pill monitoring device).
Multilevel Gaming Adherence Intervention
Combination of electronic medication monitoring device with Information-Motivation-Behavior based mobile gaming application tailored for those living with HIV and adherence-based text messages
Treatment as Usual +
TAU+ participants will receive the Treatment As Usual + intervention, which includes receiving a non-HIV related mobile game and an electronic pill monitoring device.
Treatment as Usual +
Combination of electronic medication monitoring device and non-HIV related mobile gaming application
Interventions
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Multilevel Gaming Adherence Intervention
Combination of electronic medication monitoring device with Information-Motivation-Behavior based mobile gaming application tailored for those living with HIV and adherence-based text messages
Treatment as Usual +
Combination of electronic medication monitoring device and non-HIV related mobile gaming application
Eligibility Criteria
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Inclusion Criteria
* English speaking
* Have started antiretroviral therapy (ART) in the last three months or restarted ART in the last three months after not taking ART for approximately six months
* Have access to a smartphone for the duration of the study
* Not involved with another HIV prevention or adherence related study
* Able to give consent/assent and not impaired by cognitive or medical limitations as per clinical assessment
* Detectable viral load
Exclusion Criteria
15 Years
30 Years
ALL
No
Sponsors
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University of Mississippi Medical Center
OTHER
Boston Medical Center
OTHER
Emory University
OTHER
Rhode Island Hospital
OTHER
Responsible Party
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Laura Whiteley
Assistant Professor
Principal Investigators
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James B Brock, MD
Role: STUDY_DIRECTOR
University of Mississippi Medical Center
Rachel Epstein, MD
Role: STUDY_DIRECTOR
Boston Medical Center
Stephen Pelton, MD
Role: STUDY_DIRECTOR
Boston Medical Center
Larry K Brown, MD
Role: STUDY_DIRECTOR
Rhode Island Hospital
Laura Whiteley, MD
Role: PRINCIPAL_INVESTIGATOR
Rhode Island Hospital
Andres Camacho-Gonzalez, MD
Role: STUDY_DIRECTOR
Emory University
Locations
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Emory University
Atlanta, Georgia, United States
Boston Medical Center
Boston, Massachusetts, United States
University of Mississippi Medical Center
Jackson, Mississippi, United States
Rhode Island Hospital
Providence, Rhode Island, United States
Countries
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References
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Palmer MJ, Henschke N, Villanueva G, Maayan N, Bergman H, Glenton C, Lewin S, Fonhus MS, Tamrat T, Mehl GL, Free C. Targeted client communication via mobile devices for improving sexual and reproductive health. Cochrane Database Syst Rev. 2020 Jul 14;8(8):CD013680. doi: 10.1002/14651858.CD013680.
Other Identifiers
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217318
Identifier Type: -
Identifier Source: org_study_id
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